Synergy Spine Solutions announced today that it received FDA premarket approval (PMA) for its Synergy Disc for 1-level indications at C3-C7.

Synergy Spine Solutions earned the FDA’s premarket approval for its Synergy Disc, according to a Feb. 27 news release. The device is approved for 1-level cervical disc replacement at C3 to C7 for ...

Please provide your email address to receive an email when new articles are posted on . Use of an artificial cervical disc from Spinal Kinetics LLC in the treatment of degenerative cervical ...

Synergy Spine Solutions®, a medical device company focused on improving the quality of life for patients undergoing spine surgery, today announced it has received U.S. Food and Drug Administration ...

Usually the first step is conservative treatment. Patients who have radicular symptoms but who do not have weakness or myelopathy can be treated conservatively. Conservative treatment can include ...

LEWISVILLE, Texas--(BUSINESS WIRE)--Orthofix Medical Inc. (NASDAQ:OFIX), a global medical device company with a spine and orthopedics focus, today announced the first patient implant in a U.S. Food ...

The motion-sparing advantages offered by a semiconstrained total disc prosthesis make it a promising alternative to discectomy and fusion for treating cervical spondylosis and degenerative disc ...

Adding to the already length list of reasons not to smoke, researchers have connected smoking to worsening degenerative disc disease in the cervical spine, according to research presented this week at ...

TA Criterion 1: The technology must have final approval from the appropriate government regulatory bodies. The Prestige® Cervical Disc (Medtronic Sofamor Danek, Memphis, TN) received FDA Premarket ...